Jaggard v. Abbott Cardiovascular Systems Inc

District Court, D. Nevada·Decided September 11, 2023·No. 3:21-cv-00360·Unknown

Opinion

RICHARD JAGGARD and JUDY JAGGARD,

Plaintiffs, Case No. 3:21-CV-00360-RCJ-CLB v. ORDER INC., a California corporation, and DOES 1 through 50, inclusive,

Defendants.

Defendant, Abbott Cardiovascular Systems Inc. (“Abbott”), brings a Motion for Summary Judgment against Plaintiffs Richard and Judy Jaggard (collectively “Plaintiffs”). (Dkt. 47). Abbott also requests permission to file the summary judgment motion under seal. (Dkt. 46). Abbott argues that summary judgment is appropriate for four reasons: (1) Plaintiffs’ suit is time barred by the statute of limitations, (2) Plaintiffs released their claims against Abbott in a previous settlement agreement, (3) the record lacks expert evidence as to causation, and (4) the record lacks evidence of any product defect recognized under Nevada law. (Dkt. 47 at 3–4). For the reasons discussed below, the Court finds that Plaintiffs have previously released their claims against Abbott, and Abbott is entitled to summary judgment in its favor. A. Injury In March of 2017, Jaggard was admitted to St. Mary’s Regional Medical Center (“St. Mary’s”) and underwent a cardiac catheterization and angioplasty to remove blockage in his coronary arteries. (Dkt. 47 at 3); (Dkt. 26 at 2). Dr. Devang Desai, M.D. (“Dr. Desai”) treated the blockages by inserting catheters and a Hi-Torque Balance Middleweight Guide Wire (“BMW Wire”), manufactured by Abbott, into Jaggard’s blood vessels using his right wrist as the entry point. (Dkt. 47 at 5–6); (see also Dkt. 47-7 at 2–3). The catheters cleared a pathway for the BMW Wire to move up the artery, through the blood vessels and to the blockage “like a rail to guide a stent to support the artery’s wall.” (Id.). Originally cleared for use in 1997, (Dkt. 47 at 4), the BMW Wire is a medical device approved under the FDA’s 510(k) process. See 21 U.S.C. § 301-399i; 21 C.F.R. 807 (requirements for 510(k) submission). The BMW Wire is “intended to facilitate the placement of balloon dilatation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).”1 The BMW Wire is “one of the most frequently used wires in interventional cardiology[.]” (Dkt. 47-15 at 6); (see also Dkt. 47-12 at 3).

In his operative notes, Dr. Desai recorded that there was “resistance” when removing the BMW Wire. (Dkt. 47-7 at 3). Dr. Desai also recorded that the tip of the BMW Wire marker had stripped off the BMW Wire but that the rest of the wire “appeared intact.” (Id.). Jaggard was then discharged from the hospital. (Dkt. 47 at 6). Roughly two weeks later, Jaggard experienced symptoms that prompted him to return to the hospital. (Id.). He continued to suffer from the same symptoms that he suffered from leading up to the procedure to clear the blockages in his arteries. (Id.). To treat his symptoms, Dr. Frank Carrea, M.D. “(Dr. Carrea”) performed another cardiac catheterization. (Id.). In doing so, Dr. Carrea discovered that, despite Dr. Desai’s observation that the BMW Wire appeared intact, a strand of the BMW Wire remained inside of Jaggard from the previous procedure. (Id.); (Dkt. 47-8 at 3); (Dkt. 47-9 at 2). During the procedure, Jaggard’s wife

1 This definition comes from the 510(k) clearance that Abbott submitted to Department of Health remained in the waiting room where a member of his medical team informed her that “they had found a wire in his heart and that the doctor would have to fill [her] in on the details.” (Dkt. 47-8 at 3). As a result of this finding, Jaggard would need another procedure to remove the “remaining portion of the wire[.]” (Dkt. 47 at 3). The following day, the head of the stent lab visited Jaggard in the hospital and “explained what happened.” (Dkt. 47-10 at 4). In the first procedure, Dr. Desai had “left behind a portion of an Abbott guide wire that had become snagged in his vasculature.” (Dkt. 47 at 3). And although Dr. Carrea was able to remove a piece of the BMW Wire, he did not remove the entire BMW Wire. (Dkt. 47-3 at 16–17); (Dkt. 47-12 at 11). This ultimately led Jaggard to seek a second opinion from Dr. Jason Rogers, M.D. (“Mr. Rogers”), who was willing to try to remove the BMW Wire and treat the blockages that Dr. Desai did not treat. (Dkt. 47-20 at 2). Dr. Rogers quickly performed a procedure removing the BMW Wire that remained in Jaggard. (Id.).

B. Previous Litigation On March 27, 2018, the Jaggards brought an action against St. Mary’s and Dr. Desai alleging that their negligence relating to the BMW Wire had caused him to suffer fear and anxiety, concern over past and future medical care, and loss of quality of life. (Dkt. 47 at 7); (Dkt. 47-16 at 7). The case resolved towards the end of 2020 when Plaintiffs settled their claims against St. Mary’s and Dr. Desai, (Dkt. 47 at 3). As part of the settlement, Plaintiffs entered into a general release and settlement agreement on February 8, 2021. (Dkt. 47-17 at 7–11). According to the agreement, the Released Parties were to include “all entities related to in or any way affiliated with Prime Healthcare and St. Mary’s Regional Medical Center, which encompass, but are not limited to, subsidiaries, affiliates and related companies, . . . health care

providers, nurses, staff, suppliers, representatives, . . . and any other persons, corporations, firms or entities on their behalf liable or allegedly liable, whether known or unknown[.]” (Id. at 7–8). Per the “General Release” clause, Plaintiffs “forever and fully release[d], discharge[d] and aquit[ted] the Released Parties from any and all claims, demands, actions, and causes of action which [Plaintiffs] currently ha[d], or may hereafter have against Released Parties, whether known or unknown, that are in any way related to or allegedly arise out of the events giving rise to the underlying litigation.” (Id. at 8–9). Binding upon and inuring to the benefit of all Released Parties, including suppliers, (id. at 9), the stated “intent” of the agreement was “to fully and finally settle and compromise any and all claims or causes of action, whether known or unknown, that [Plaintiffs] has or might have against Released Parties . . . that are in any way related to or arise out of the events giving rise to the underlying litigation.” (Id. at 8). Finally, the agreement stipulates that it is to be governed by Nevada law. (Id. at 10).

A court must grant summary judgment when “the movant shows that there is no genuine dispute as to any material fact and the movant is entitled to judgment as a matter of law.” Fed. R. Civ. P. 56(a). Material facts are those which may affect the outcome of the case. See Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 248 (1986). A dispute as to a material fact is genuine if there is sufficient evidence for a reasonable jury to return a verdict for the nonmoving party. See id. In determining summary judgment, a court uses a burden-shifting scheme. “When the party moving for summary judgment would bear the burden of proof at trial, it must come forward with evidence which would entitle it to a directed verdict if the evidence went uncontroverted at trial.” C.A.R. Transp. Brokerage Co. v. Darden Rests., Inc., 213 F.3d 474, 480 (9th Cir. 2000) (citation and internal quotation marks omitted). In contrast, when the nonmoving party bears the

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Jaggard v. Abbott Cardiovascular Systems Inc, (D. Nev. 2023).

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